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荧光定量PCR检测FGFR2基因多态性与雌激素受体阳性乳腺癌的相关性

[Association of FGFR2 gene polymorphism with estrogen receptor positive breast cancer detected by fluorescent quantitative PCR].

作者信息

Ren Li, Zhang Bin, Cao Xu-chen, Chen Ying, Ge Jie

机构信息

Department of Clinical Laboratory, Cancer Hospital, Tianjin Medical University, Tianjin, 300060 PR China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):445-8. doi: 10.3760/cma.j.issn.1003-9406.2010.04.019.

Abstract

OBJECTIVE

To investigate the association of fibroblast growth factor receptor 2 gene (FGFR2) rs2981582 polymorphism with breast cancer in Chinese women.

METHODS

A case-control study was performed in 936 breast cancer patients and 471 patients with benign breast diseases by using a novel fluorescent quantitative PCR method.

RESULTS

The numbers and frequencies of genotypes CC, CT, and TT in the control group were 234(49.68%), 181(38.43%) and 56(11.89%) respectively. The numbers and frequencies of genotypes CC, CT, and TT in the breast cancer group were 426(44.56%), 400(41.84%) and 130(13.60%) respectively. And no significant difference was found between the two groups (P=0.183). However, stratified analysis found that the numbers and frequencies of genotypes CC, CT, TT in the estrogen receptor(ER) positive subgroup of breast cancer patients were 189(41.27%), 202(46.12%) and 67(14.63%) respectively, and significant difference was observed compared with control group (P=0.035).

CONCLUSION

Association was found in the single nucleotide polymorphism(SNP) of the rs2981582 locus of intron 2 in FGFR2 gene between the ER positive breast cancer patients and control patients with benign breast diseases. The fluorescent quantitative PCR is a specific, easy-to-operate, low-expense method and is suitable for SNP detection in large scale samples.

摘要

目的

探讨中国女性成纤维细胞生长因子受体2基因(FGFR2)rs2981582多态性与乳腺癌的相关性。

方法

采用新型荧光定量PCR方法,对936例乳腺癌患者和471例乳腺良性疾病患者进行病例对照研究。

结果

对照组中CC、CT和TT基因型的数量及频率分别为234例(49.68%)、181例(38.43%)和56例(11.89%)。乳腺癌组中CC、CT和TT基因型的数量及频率分别为426例(44.56%)、400例(41.84%)和130例(13.60%)。两组间差异无统计学意义(P=0.183)。然而,分层分析发现,乳腺癌患者雌激素受体(ER)阳性亚组中CC、CT、TT基因型的数量及频率分别为189例(41.27%)、202例(46.12%)和67例(14.63%),与对照组相比差异有统计学意义(P=0.035)。

结论

FGFR2基因内含子2的rs2981582位点单核苷酸多态性(SNP)与ER阳性乳腺癌患者及乳腺良性疾病对照患者之间存在相关性。荧光定量PCR是一种特异性强、操作简便、费用低廉的方法,适用于大规模样本的SNP检测。

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